Insulin isophane biphasic porcine 30/70 100units/ml suspension for injection 1.5ml cartridges
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Hypurin Porcine 30/70 Mix 100units/ml suspension for injection 1.5ml cartridges
WHO defined daily dose (DDD)
40 unit
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 5 · Randomised trials: 1 · 1979–2026
Showing the 50 most relevant studies, sorted by most relevant.
Hemmingsen B, Metzendorf MI, Richter B
2021
- Myocardial Infarction
- Diabetes Mellitus, Type 1
- Hypoglycemia
B. M. Frier, D. Russell‐Jones, T. Heise
Diabetes, Obesity and Metabolism, 2013
G. Cruise, O. Hegre, F. Lamberti, et al.
Cell Transplantation, 1999
Vardi M, Jacobson E, Nini A, et al.
2008
- Diabetes Mellitus, Type 1
- Insulin
- Insulin, Long-Acting
Dhatariya K, Levy NA, Stubbs D, et al.
2025
- Diabetes Mellitus
- Insulin
- Hypoglycemic Agents
Diabetes mellitus is characterised by an elevated blood glucose concentration. Over the last two decades, a plethora of new agents have emerged to help treat the condition, of which several classes of agent have been shown to reduce the risk of cardiovascular morbidity and mortality. In addition, there have been several developments in the pharmacology of insulin, improving the pharmacokinetics and pharmacodynamics of insulin analogues to better mimic physiological insulin concentrations in the liver, skeletal muscle, and other tissues. Furthermore, the technologies used to deliver insulin and measure glucose have improved; for example, in the UK, hybrid closed loop systems are now the standard of care for people with type 1 diabetes mellitus. This review focuses on insulin and insulin delivery. We consider the history of insulin development and the pharmacology of newer insulin analogues. We also describe the novel technologies available and the considerations that need to be made by anaesthetists, surgeons, and other members of the perioperative team when looking after someone with diabetes mellitus on these insulins, or using these devices, to ensure safe care and the avoidance of complications.
Abstract licence: CC BY
Karl Horvath, Klaus Jeitler, Andrea Berghold, et al.
Cochrane Database of Systematic Reviews, 2007
A. Garber
Drugs, 2012
Ajay Kumar
Indian Journal of Endocrinology and Metabolism, 2016
Kjeld Hermansen, Michele Colombo, Heidi Storgaard, et al.
Diabetes Care, 2002
Richter B, Bongaerts B, Metzendorf MI
2023
- Insulin
- Drug Stability
- Drug Storage
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.